Garcia-Martin C, Baldomà L, Badía J, Aguilar J
Department of Biochemistry, School of Pharmacy, University of Barcelona, Spain.
J Gen Microbiol. 1992 Jun;138(6):1109-16. doi: 10.1099/00221287-138-6-1109.
The precise location of the rhaT gene, encoding rhamnose permease, has been established between sodA and rhaC at 3605-3607 kb of Kohara's physical map, which corresponds to 88.4 min on the Escherichia coli chromosomal map. The dependence of the activity of the rhaT product on the function of rhaC, the rhamnose operon regulatory gene, was established by measuring rhamnose transport in wild-type and rhaC-deficient strains. The sequence of the sodA-rhaC interval displayed a single ORF corresponding to rhaT, which is transcribed counterclockwise on the E. coli chromosome. The ORF was shown to be preceded by a ribosome binding consensus sequence and a catabolite repression protein consensus sequence. The derived amino acid sequence displayed very low homology with any other permease and was clearly dissimilar to the homologous group formed by the xylose, arabinose, galactose and several glucose transporters. Analysis of the rhaT primary sequence identified potential membrane-spanning regions, possibly defining a protein structure model different from the one corresponding to the above-mentioned homologous group.
编码鼠李糖通透酶的rhaT基因的精确位置已确定在Kohara物理图谱的3605 - 3607 kb处,位于sodA和rhaC之间,这对应于大肠杆菌染色体图谱上的88.4分钟。通过测量野生型和rhaC缺陷型菌株中的鼠李糖转运,确定了rhaT产物的活性对鼠李糖操纵子调节基因rhaC功能的依赖性。sodA - rhaC区间的序列显示出一个与rhaT相对应的单一开放阅读框(ORF),它在大肠杆菌染色体上逆时针转录。该ORF之前有一个核糖体结合共有序列和一个分解代谢物阻遏蛋白共有序列。推导的氨基酸序列与任何其他通透酶的同源性非常低,并且与由木糖、阿拉伯糖、半乳糖和几种葡萄糖转运蛋白形成的同源组明显不同。对rhaT一级序列的分析确定了潜在的跨膜区域,这可能定义了一种与上述同源组不同的蛋白质结构模型。